Geoff C. Nicholson

Association of functionally different RUNX2 P2 promoter alleles with BMD (2006)

Doecke, James D, Day, Christopher J, Stephens, Alexandre S, Carter, Shea L, Van Daal, Angela, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of functionally different RUNX2 P2 promoter alleles with BMD (2006)

Doecke, James D, Day, Christopher J, Stephens, Alexandre SJ, Carter, Shea L, Van Daal, Angela, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of functionally different RUNX2 P2 promoter alleles with BMD (2006)

Doecke, James D, Day, Christopher J, Stephens, Alexandre SJ, Carter, Shea L, Van Daal, Angela, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of Functionally Different RUNX2 P2 Promoter Alleles with BMD (2006)

Doecke, James David, Day, Christopher, Stephens, Alexandre, Carter, Shea L, Daal, Angela Van, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of Functionally Different RUNX2 P2 Promoter Alleles with BMD (2006)

Doecke, James David, Day, Christopher, Stephens, Alexandre, Carter, Shea L, Daal, Angela Van, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of functionally different RUNX2 P2 promoter alleles with BMD (2006)

Doecke, James D, Day, Christopher J, Stephens, Alexandre SJ, Carter, Shea L, Van Daal, Angela, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of Functionally Different RUNX2 P2 Promoter Alleles with BMD (2006)

Doecke, James David, Day, Christopher, Stephens, Alexandre, Carter, Shea L, Daal, Angela Van, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of functionally different RUNX2 P2 promoter alleles with BMD (2006)

Doecke, James D, Day, Christopher J, Stephens, Alexandre SJ, Carter, Shea L, Van Daal, Angela, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

Association of Functionally Different RUNX2 P2 Promoter Alleles with BMD (2006)

Doecke, James David, Day, Christopher, Stephens, Alexandre, Carter, Shea L, Daal, Angela Van, Kotowicz, Mark A, ...

RUNX2 gene SNPs were genotyped in subjects from the upper and lower deciles of age- and weight-adjusted femoral neck BMD. Of 16 SNPs in RUNX2 and its two promoters (P1 and P2), only SNPs in the P2...

NFAT expression in human osteoclasts (2005)

Day, Chris, Kim, Michael Soo Ho, Lopez, Carolina M., Nicholson, Geoff C., Morrison, Nigel Alexander

Nuclear factor of activated T-cells cytoplasmic (NFATc) is a family of transcription factors originally identified in T-cells. The gene family is currently known to have four members (NFATc1 through...

Gene Array Identification of Osteoclast Genes: Differential Inhibition of Osteoclastogenesis by Cyclosporin A and Granulocyte Macrophage Colony Stimulating Factor (2004)

Day, Chris, Kim, Michael Soo Ho, Stephens, Sebastien Robert, Simcock, Wendy Elizabeth, Aitken, Cathy J., Nicholson, Geoff C., ...

Treatment of adherent peripheral blood mononuclear cells (PBMCs) with macrophage colony stimulating factor (M-CSF) and receptor activator of NF-B ligand (RANKL) stimulates the formation of...

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease (2002)

Lucas, Gavin J A, Daroszewska, Anna, Mangion, Jon, Olavesen, Mark, Cundy, Tim, ...

Paget's disease of bone (PDB) is a common disorder characterized by focal abnormalities of increased and disorganized bone turnover. Genetic factors are important in the pathogenesis of PDB, and in...

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease (2002)

Hocking, Lynne J., Lucas, Gavin J.A., Daroszewska, Anna, Mangion, Jon, Olavesen, Mark, Cundy, Tim, ...

Paget's disease of bone (PDB) is a common disorder characterized by focal abnormalities of increased and disorganized bone turnover. Genetic factors are important in the pathogenesis of PDB, and in...

Genomewide Search in Familial Paget Disease of Bone Shows Evidence of Genetic Heterogeneity with Candidate Loci on Chromosomes 2q36, 10p13, and 5q35

Hocking, Lynne J., Herbert, Craig A., Nicholls, Rosie K., Williams, Fiona, Bennett, Simon T., Cundy, Tim, ...

Paget disease of bone (PDB) is a common disorder characterized by focal abnormalities of increased and disorganized bone turnover. Genetic factors are important in the pathogenesis of PDB, and...

Genomewide Search in Familial Paget Disease of Bone Shows Evidence of Genetic Heterogeneity with Candidate Loci on Chromosomes 2q36, 10p13, and 5q35

Hocking, Lynne J., Herbert, Craig A., Nicholls, Rosie K., Williams, Fiona, Bennett, Simon T., Cundy, Tim, ...

Paget disease of bone (PDB) is a common disorder characterized by focal abnormalities of increased and disorganized bone turnover. Genetic factors are important in the pathogenesis of PDB, and...